Diagnostic Kit for Detecting Pulmonary and Extra Pulmonary

ABSTRACT

A diagnostic kit for detecting pulmonary and extra pulmonary tuberculosis comprising a test card “TB Screen” coated with a hydrophobic material, antigen suspension, positive and negative control.

FIELD OF THE INVENTION

This invention relates to a diagnostic kit for detecting pulmonary & extra pulmonary tuberculosis.

BACKGROUND OF THE INVENTION

The conventional methods for detecting tuberculosis is time consuming & labour consuming AFB staining is considered to be insensitive (requiring 10,000 organism/ml of sputum for smear positive result with 100× microscope, refer Todar's Text Book of Bacteriology Online). ELISA-KP 90 is also known to be of low sensitivity and specificity and specificity (cut-off value >1.0 +ve, and <0.8 −ve test result) and requires sophisticated infrastructure as also the hypersensitivity based Tuberculin Skin Test (Montaux test) which lacks sensitivity and specificity In BOG vaccinated patient (Constantin P. et. al., Inf & Imm 1998; 66). In the same way MYCODOT is inconvenient for HIV correlated individuals (refer G. R. Somi et. al., Int J Tubercle and Lung Disease, 19999, vol 3) and Bactec-460 and Roche molecular system PCR based product) are though sensitive requires very costly infrastructure and technical expertise.

OBJECTS OF THE INVENTION

An object of this invention is to propose a diagnostic kit for detecting tuberculosis.

A further object of this invention is to propose a diagnostic kit which is economical and easy to handle.

A still further object of this invention is to propose a diagnostic kit based on liposome agglutination.

Another object of this invention is to propose a diagnostic kit which is sensitive and specific as it is based on a specific antigenic, antibody reaction.

Still another object of this invention is to propose a diagnostic kit which helps in fast detection of tuberculosis.

BRIEF DESCRIPTION OF THE INVENTION

According to this invention there is provided a diagnostic kit for detecting pulmonary & extra pulmonary tuberculosis comprising a test card “TB Screen” coated with a hydrophobic material, antigen suspension, positive and Negative control.

In accordance to this invention there is provided a method of detecting tuberculosis using the kit comprising

applying positive control, negative control & test sample each in circular motion on the test card coated with hydrophobic material adding said antigen suspension to each of the positive, negative & test sample to interpart the results, clumping of specific antigen and anti body as dark blue agglutination was observed in positive control and the test sample which contain the active tuberculosis Infection.

DETAILED DESCRIPTION OF THE INVENTION

The Mycobacterium tuberculosis H₃₇Rv (ATCC-27294) strains was grown on Sautons media till late log phase (2-3 month) and cells were harvested by centrifugation (5000,-10,000 g for 10-20 min) at 4-10 C, the pellet was washed with PBS (pH 7.2-7.6), resuspended with TEN buffer PH 8.0-8.5 (10 mM Trs HC1, 1 mM EDTA, 100 mM NaCl) and heat inactivated at 70-80C (waterbath) for 30-45 min. followed by sonication. The glycolipid antigens were extracted according to the procedure mentioned in the literature (Reggiardo et al., 1974; Bisen P. S. et al., 2003) with the slightly modification in the procedure. The lypolized Mycobacterial powder (10-15 g was taken into a glass reagent bottle and to it 100-150 ml of chloroform and methanol mixture (2:1) was added. This was stirred at room temperature for 50-60 min. and filtered through whatman filter paper No 1. The ⅕ volume of 0.7°% KCl (20.0 ml) was added to the filtrate and was shaken for 5.6 times. The suspension was transferred to a separating funnel and kept at 2-8° C. for overnight till two distinct layers were separated. The lower organic phase was washed with ⅙ volume of washing solvent (C:M:W:3:48:47) in similar manner by keeping at 2-8° C. for overnight. The upper aqueous phase was removed and lower organic phase was retained after filtering. The organic phase was dried by evaporating the solvent in rotatory solvent evaporator at 40-50° C. The moisture was removed by flushing the dried mixture with nitrogen gas. Neutral lipids were removed from the dried mixture by adding 300-600 ml of chilled acetone vortexing it for 10-20 min and filtering it through whatman No. 1. This step was repeated till the lipids in the flask became whitish or colorless. This was filtered through whatman No. 1 and the filtrate was discarded. The lipids present on the filter paper were dissolved with C:M (2:1) and transferred to the R.B flask. Solvent was rotary evaporated under reduced pressure at 40-50° C. The crude preparation was reconstituted in 10-16 ml of C:M (2:1) and stored at −20° C. for further use.

Purification of Antigen(s):

The Silica gel H activated at 100-110° C. for 1-1.30 hrs. (Hot air oven) was packed with, glass column (2.6×30 cm) with manual tapping and known quantity of crude material (1 g/5 ml, stock) was loaded on either side of the column. The column was run ascending on chromatographic jar (4.5×25 cm) with purification solvent, 160-200 ml (mobile phase) in a ratio of 66:25:4 (C:M:W)^(7,8) at room temperature to run the column till other it reached the end. The column was removed from the chromatographic jar and placed on fume hood to evaporate the solvent from the column. The 1 cm length of each fraction was carefully scrapped using clean rod so as to get the separate molecules which were adsorbed with the silica gel depending upon the mobility and Retardation Factor (RF) value (46.6, 63.4, 68.3, 67.2 and 72.4%) of individual molecule. The individual fraction was collected into clean dry glass test tubes which were labeled with respective fraction number, Ten ml of extraction solvent (mixture of chloroform: Methanol 2:1) was added to each test tubes and kept at room temperature for 30-40 min. The purity of eluted material was analyzed by TLC and the selected fraction were further filtered through Whatman filter paper No. 1 to remove the silica gel from the samples. The pure fractions were pooled and these were characterized by conventional methods (Immuno-staining on TLC, ELISA and by Liposome).

Method for the Construction of Liposomal Antigens:

Liposome was prepared as described previously (Bangham A. D et. al. 1965) with minor modification in the procedure, in brief Phophotidylcholine 100-160 mg; cholesterol, 450-500 mg (Sigmas USA); antigenic suspension (Cocktial) 10-20 mg; and dye 50-100 μl (1.0% sudan black B in Chloroform) were taken in a pre-dried round bottom flask. Solvent was evaporated by rotatory vacuum evaporator under reduced pressure. The dried contents were dissolved in 40-50 ml of absolute alcohol (99.9% Hyman, Germany) and were kept at 4°10° C. for 1-1.30 hrs. Sucrose solution (4-8 ml; 150 Mm) was taken in a polypropylene centrifuge tube (capacity 35 ml) and to that 4-5 ml of pre-prepared alcoholic antigen suspension was gently added while vortexing. The tubes were kept over night at 4° C.-10C for liposome swelling, vortexed with 10-15 ml of PBS (pH 6.5) buffer and centrifuged at 10,000 g for 10-20 min (Beckman, USA). The supernatant was discarded and the pellet was resuspended with 20-30 ml of 12 buffer, pH 7.2 (NaH₂PO₄.2H₂O, 10 mM; KH₂PO₄, 10 mM; EDTA, 10 mM; Choline Chloride, 10% and Thiomersol, 0.1%). This was stored at 4° C.-10C for further use and utilized as antigen reagent for the kit.

Preparation of Phosphatidylcholine:

Phosphatidylcholine (PC) was prepared in house to reduce the cost of the test. Those skilled in the art are aware of purification of PC from egg yolk and it's final estimation (Sunamoto, J. et al 1978). In brief, 25 eggs were taken and albumin portions were removed. The collected yolk was extracted with 750 ml of Chloroform: Methanol (2:1) by stirring for half an hour. Filtered through Whatmann no. 1. The filterate was deproteinised with one fifth volume of 0.7% of KC1. To the organic layer so obtained, washing was performed with 3:48:47 of Chloroform:methanol: water. Moisture was removed by using benzene. Solvent was evaporated with the aid of rotary vacuum evaporated with the aid of rotary vacuum evaporator and a dried film of lipid was obtained. Neutral lipids were removed as described above with acetone. Empty weight of round bottom flask was taken (Wa). Flask was weighed along with the dried lipid film. 37.5 g of crude lipid was Isolated. The crude product was further purified by silica gel H chromatography and purified PC was characterized by Thin layer chromatography and PC estimation was performed as known in the prior art (Sunamoto, J. et al 1978).

Preparation of Positive Control for Test:

1 mg of Mycobacterium tuberculosis pellet was taken after centrifugation of mycobacterial growth in Sauton's medium. The pellet was washed twice with 1×PBS to get rid of media remnants. The pellet was then suspended in 4 ml of 1× Phosphate buffered saline. 4-8 acid washed beads of 5 mm diameter was added to the above. The sample was vigorously shaken for 10 mm on a vortex. The suspension obtained was mixed with an equal volume of Freunds Incomplete Adjuvant. The mixture was squeezed through 22 g needle repeatedly till it reaches a desired level. 100 ul of suspension was inoculated to a young rabbit of 2-8 months. A number of rabbits were inoculated in the same manner.

Rabbits were bled after one month and serum was obtained. The reactivity of serum was checked with the antigen suspension as described in the test procedure given in next paragraph. The reactivity titer was checked. A booster administration of the antigen (50 ul) was again repeated. An enhanced titer of about 1.64 to 1:128 was obtained after about seven days of booster dosage. Best reactivity titer was obtained. The serum was diluted to optimum reactivity titer in 1× PBS and 0.1% azide was added as preservative so as to contain any contamination. The stock was frozen till used/dispensed in vials.

The 4-6 month old Rabbits were immunized with the above antigens and bled 110 periodically and used for positive control to be provided with the kits, where as normal young Rabbit were used for Negative control.

Method of Testing:

All the components such as positive control, negative control antigen suspension and sample to be tested were brought to room temperature before performing the experiments. Positive control, negative control and test sample (25 μl each) were added in circular motion, as demonstrated on the test card. The above samples were spread by using separate sticks in round conjugation, 26 μl of liposome antigen was added to it and the card was gently swirled for 4 min.

Freshly procured or frozen test serum samples (25 μl) were spread evenly inside the circular zone of hydrophobic material coated plastic slide. For convenience, zone 1 and 2 were spread with the positive (anti-rabbit serum) and negative control (normal rabbit serum) and negative control (normal rabbit serum) respectively, to interpret the results. The antigenic suspension (25 μl) was added to each circular zone including zone 1 and 2 and the card was manually swirled for 4 min. The clumping of specific antigen and antibody as dark blue agglutination were observed in positive control as well as in those samples which contain antibodies against mycobacterial glycolipid with active tuberculosis infection. No clumping on the card whereas, indicated a negative result. The peripheral drying on the circular zone indicated indiscriminate results, which require further confirmation within 16-30 days, as these samples contained undetectable level of antigen concentration in the specimens.

EXAMPLE 1

Sera:—

Patient sera from outdoor patient departments (OPD) from different hospitals of India were enrolled in the present study to cover maximum population diversity. The patients were diagnosed on the basis of clinical and radiological evaluation as well as smear staining and sputum culture of samples. None of the patients was completely treated. Both extrapulmonary as well as pulmonary tuberculosis sera were included in the study. A total of three hundred and twenty four (324) tuberculosis sera were studied.

Sera from healthy individuals without any clinical symptoms of TB were included as negative controls to evaluate specificity criterion of the test. Most of these were obtained from BCG vaccinated subjects. The non-TB sera generally belonged either to healthy individuals or to patients suffering from a variety of diseases other than tuberculosis. The sera were stored frozen and were used within 1 year from the time, they were taken. Also five hundred and eleven (511) tuberculosis negative sera were included in this testing. The details of criteria used in selection of sera is as follows; Smear Negative, Culture Positive pulmonary cases 52 Smear Positive, Culture Positive, pulmonary cases 180 Extrapulmonary, Culture Positive cases 35 Relapse pulmonary cases 57 Drug treated, clinically negative cases 60 Healthy household contacts 50 BCG vaccinated children 15 Hepatitis B positive samples 15 Sera from common infections other than TB 27 Normal human sera 344

EXAMPLE 2

In House Evaluations:—

An overall sensitivity of 98.68% was obtained using a panoply of three hundred and twenty four tuberculosis sera, out of which 20 sera showed indiscriminate results. Indiscriminate sera were not included in the sensitivity and specificity calculations, as per method adopted by WHO. An overall specificity of 98.78% was obtained using five hundred and eleven non-tuberculosis sera.

Sera from 15 children who were recently immunized with BCG were tested for any cross-reactivity of the test with vaccination. None of the sera yielded positive results, thereby indicating the suitability of the test in BCG vaccinated populations such as india and others.

15 cases of Hepatitis B positive samples were evaluated for cross reactivity. There was no reaction in any of the sera tested. 4 Hepatitis B sera were tested with the kit at Hopkins Research Institute, Bombay with nil reactivity (not included in inhouse study table).

Out of 27 sera from other common infections, 25 showed clear negative and rest two showed indiscriminate results. There was a need to chase these subjects for progression to tuberculosis, but unfortunately, it could not be done. Indeterminate results were omitted from specificity and sensitivity calculations.

Results of inhouse studies are tabulated as follows: TABLE 1 STUDIES PERFORMED ON TUBERCULOSIS POPULATION SERA DETAILS RESULTS Number of tuberculosis sera tested = 324 positive = 300 negative = 4 indeterminate = 20** SENSITIVITY = 98.68% Smear Negative, Culture Positive pulmonary positive = 47 cases - 52 negative = 2 indeterminate = 3 Smear Positive, Culture Positive, pulmonary positive = 175 cases - 180 negative = — indeterminate = 5 Extrapulmonary cases, Culture Positive - 35 posltive = 28 negative = 2 indeterminate = 5 Relapse pulmonary cases - 57 positive = 50 negative = — indeterminate = 7 **indiscriminate samples were not included in Sensitivity & specificity calculations as per WHO methodology

TABLE 2 STUDIES PERFORMED ON NON-TUBERCULOUS SERA Number of non-TB sera tested = 511 positive = 488 negative = 6 indeterminate = 17** SPECIFICITY = 98.78% 5. Drug treated, clinically negative positive = — cases - 60 negative = 51 indeterminate = 9 6. Healthy household contacts - 50 positive = — negative = 50 indeterminate = — 7. BCG vaccinated children - 15 positive = — negative = 15 indeterminate = — 8. Hepatitis B positive samples - 15 positive = — negative = 15— indeterminate = 9. Sera from common infections positive = — (Not TB) - 27 negative = 25 indeterminate = 2 10. Normal human sera - 344 positive = 6 negative = 332 indeterminate = 6 **indiscriminate samples were not included in Sensitivity & specificity calculations as per WHO methodology

Excellent results were obtained when using fresh sera from subjects under investigation. Frozen sera can be tested after thawing, but repeated freeze thawing of samples might affect the outcome. 

1-10. (canceled) 11: A diagnostic kit for detecting pulmonary and extra pulmonary tuberculosis, comprising a test card “TB Screen” coated with a hydrophobic material, an antigen suspension, a positive and a negative control. 12: The kit as claimed in claim 11, wherein said antigen suspension is a liposome antigen and said test card is a plastic slide. 13: The kit as claimed in claim 11, wherein said negative control is prepared from the blood of a normal young rabbit. 14: The kit as claimed in claim 11, wherein said positive control is prepared from a 4 to 6 month old rabbit which is immunized with mycobacterium antigens and bled periodically. 15: A method of detecting tuberculosis using a kit comprising applying a positive control, a negative control and a test sample, each in circular motion on a test card coated with a hydrophobic material; adding an antigen suspension to each of the positive, negative and test sample to interpret the results, wherein clumping of a specific antigen in the suspension and an antibody is observed as dark blue agglutination in the positive control and the test sample which contains the active tuberculosis infection. 16: The method as claimed in claim 15, wherein said antigen suspension is a liposome antigen. 17: The method as claimed in claim 16, wherein the lipid antigen for positive control is prepared comprising the steps of: growing Mycobacterium tuberculosis H₃₇Rv (ATCC-27294) strain on Sautons media; harvesting cells in the media by centrifugation at 4° to 10° C.; subjecting said cells to the step of sonication; extracting the antigens from said cells; adding chloroform and methanol mixture (2:1) to said antigens with stirring at room temperature; and subjecting the mixture to the step of filtration; wherein the suspension thus obtained is transferred into a separating funnel and kept overnight until two distinct layers are separated, an upper aqueous phase is removed and the lower organic phase retained after filtration, said organic phase being dried by evaporating the solvent to obtain the lipid and subjecting said lipid to the further step of purification. 18: The method as claimed in claim 15, wherein said antigen suspension is prepared comprising the steps of: adding phophotidylcholine, cholesterol, lipid antigens and dye in a flask and evaporating the solvent layer in a vacuum evaporator; dissolving the dried contents thus obtained in absolute alcohol at 4° to 10° C. for 1 to 2 hours to produce the antigen suspension; adding said antigen suspension to a sucrose solution with continuous stirring and keeping said suspension at 2° to 8° C. overnight; subjecting said suspension to centrifugation and discarding the supernatant; and suspending the pellet obtained into a buffer and stirring the same at 4° to 10° C. 19: The method as claimed in claim 16, wherein said lipid antigen is further purified using column chromatography. 20: The method as claimed in claim 18, wherein said buffer comprises NaH₂PO₄2H₂O, KH₂PO₄, EDTA, Choline Chloride and Thiomersol. 21: The method as claimed in claim 18, wherein said dye is Sudan Black in chloroform. 